• Bulletin of the Korean Chemical Society
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• v.12 no.3
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• pp.265-270
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• 1991

Theoretical calculations on the stabilization energies of framework atoms in hydrolyses Co(Ⅱ )-exchanged zeolite A were made using some potential energy functions and optimization program. The protons which are produced by hydrolysis of $[Co(H_2O)_n]^{2+}$ ion in large cavity showed a tendency to attack the framework oxygen atom O(1) preferentially, and the oxygen atom O(4) within OH- ion was coordinated at Al atom. The weakness of bonds between T(Si, Al) and oxygen by attack of proton and too large coordination number around small aluminum atom will make the framework of Co(Ⅱ)-exchanged zeolite A more unstable. The stabilization energy of $Co_4Na_4$-A framework (- 361.57 kcal/mol) was less than that of thermally stable zeolite A($Na_{12-}$A: - 419.68 kcal/mol) and greater than that of extremely unstable Ba(Ⅱ)-exchanged zeolite A($Ba_{6-}$A: - 324.01 kcal/mol). All the data of powder X-ray diffraction, infrared and Raman spectroscopy of Co(Ⅱ)-exchanged zeolite A showed the evidence of instability of its framework in agreement with the theoretical calculation. Three different groups of water molecules are found in hydrated Co(Ⅱ )-exchanged zeolite A; W(Ⅰ) group of water molecules having only hydrogen-bonds, W(Ⅱ) group water coordinated to $Na^+$ ion, ans W(Ⅲ) group water coordinated to Co(Ⅱ) ion. The averaged interaction energy of each water group shows the decreasing order of W(Ⅲ)>W(Ⅱ)>W(Ⅰ).

• Korean Journal of Soil Science and Fertilizer
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• v.28 no.4
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• pp.340-349
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• 1995

Effects of the zeolite particle size on the soil chemical properties and on rice growth was investigated on the pot with the loamy sand (Sadu series) and silty clay loam(Paju series) soils. All the zeolite treatments brought the increase of unhulled grain yield on the both loamy sand and silty clay loam soils. Unhulled grain yield increased with increasing the amount of zeolite applied and with decreasing the amount of particle size of zeolite applied on both soils. Unhulled grain yield increased significantly by 11.1% (22.79g/head) with 2ton/10a of smaller than $106{\mu}m$ size zeolite on the loamy sand soil and on the silty clay loam soil, yield increased by 9.3% (24.98g/head) with 1.5ton/10a of smaller than $106{\mu}m$ size zeolite. CEC, pH and contents of exchangeable cations of the soil after experiment were raised by increasing the amount of zeolite and also by decreasing the particle size of zeolite at both soil. At the heading stage, the zeolite treatments improved the growth of rice plant compared to control. The nutrient contents(T-N, Ca, Mg, K, Na), except phosphorus, in the rice plant grown on the zeolite treated soils were higher than control plot.

• Applied Chemistry for Engineering
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• v.22 no.4
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• pp.423-428
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• 2011

Hydration characteristics of cement containing zeolite mined at Daepo in Gyeongbuk province were studied for use as a mineral admixture. The cement paste containing zeolite was characterized by the measurement of heat evolution, XRD, EDS, nitrogen adsorption and mercury intrusion porosimetry. The cement paste containing zeolite exhibited tendencies toward acceleration of paste setting and promotion of cement hydration with the increase of zeolite content. The flow of mortar containing zeolite strongly reduced with increase of zeolite content. Compressive strength of the mortar containing zeolite increased very rapidly at an early age in comparison with plain mortar. These results would be related to aluminum species escaped from zeolite particles during the alkali dealumination of zeolite by the hydration process of cement.

• Journal of Applied Biological Chemistry
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• v.42 no.1
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• pp.25-28
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• 1999

For investigating the effectiveness of Korean natural zeolite for removal of $NH_4{^+}$ in waste waters containing $NH_4{^+}$ and $Cu^{2+}$, the adsorption of $NH_4{^+}$ and $Cu^{2+}$ by three Korean natural zeolite samples, which contained mordenite and/or clinoptilolite, was measured by adding solutions containing $NH_4{^+}$ and $Cu^{2+}$ or both at a concentration range from 1 to 7 mmol(+)/L of each cation. In the solutions, the zeolite samples adsorbed more amounts of $NH_4{^+}$ than $Cu^{2+}$. By seven successive equilibrations, Korean natural zeolites adsorbed $NH_4{^+}$ corresponding to 23~33% of those cation exchange capacity from the solution containing both $NH_4{^+}$ and $Cu^{2+}$ at 3 mmol(+)/L of each cation. Whereas, the corresponding adsorption of $Cu^{2+}$ was 17-27% of the CEC. Korean natural zeolite exhibited selectivity for $NH_4{^+}$ but not for $Cu^{2+}$. Nevertheless, it using as a soil amendment after removing of $NH_4{^+}$ in waste waters should be carefully controlled on the application rate.

• Nuclear Engineering and Technology
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• v.49 no.3
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• pp.556-561
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• 2017

Serving as an excellent adsorbent and inorganic ion exchanger in the water purification field, zeolite 4A has in this work presented a strong capability for purifying radioactive waste, such as $Sr^{2+}$, $Cs^+$, and $Co^{2+}$ in water. During the processes of decontamination and decommissioning of suspended solids and organics in low-level radioactive wastewater, the purification performance of zeolite 4A has been studied. Under ambient temperature and neutral condition, zeolite 4A absorbed simulated radionuclides such as $Sr^{2+}$, $Cs^+$, and $Co^{2+}$ with an absorption rate of almost 90%. Additionally, in alkaline condition, the adsorption percentage even approached 98.7%. After conducting research on suspended solids and organics of zeolite 4A for the treatment of radionuclides, it was found that the suspended clay was conducive to absorption, whereas the absorption of organics in solution was determined by the species of radionuclides and organics. Therefore, zeolite 4A has considerable potential in the treatment of radioactive wastewater.

• Korean Journal of Environmental Agriculture
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• v.26 no.3
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• pp.259-266
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• 2007

Enormous amount of zeolite by-products as a fine powder have been produced while manufacturing commercial zeolite products. Granulation of the zeolite by-products is necessary in order for them to be recycled as soil conditioners or absorbent for various environmental contaminants due to the limitations inherent from their physical properties. We granulated the zeolite powders using Portland cement as a cementing agent and characterized the physical and chemical properties of the granulated zeolite product. The experimental natural zeolite had a Si/Al ratio of 4.8 and CEC of 68.1 $cmol_c\;kg^{-1}$. The X-ray diffractometry (XRD) revealed that clinoptilolite and mordenite were the major minerals of natural zeolite. Smectite, feldspar and quartz also existed as secondary minerals. Optimum conditions of granulated zeolite production occurred when natural zeolite was mixed with Portland cement at a 4:1 ratio and granulated using the extruder, left to harden for one month at $25^{\circ}C$ and treated at $400^{\circ}C$ for 3 hours. The wide spectra of XRD revealed that the granulated zeolite had amorphous oxide minerals. The alkali- or thermal-treated natural zeolite exhibited pH-dependent charge properties. The major minerals of the granulated zeolite were clinoptilolite, mordenite and tobermorite. The buffering capacity and charge density of the granulated zeolite were greater than those of natural zeolite.

• Clean Technology
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• v.26 no.4
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• pp.263-269
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• 2020

Zeolite was synthesized hydrothermally using the water-treatment sludge, and the effects of various synthesis parameters like reaction temperature, reaction time, and Na2O/SiO2 molar ratio on the crystallization of zeolite were investigated. Crystal structure, physical property, and thermal stability of zeolite crystals were characterized by X-ray powder diffraction, FTIR spectroscopy, BET nitrogen adsorption, and TGA measurements. The removal efficiencies of nitrogen in ammonia, heavy metal ions, and TOC were calculated to evaluate zeolite's adsorption capacity. The primary chemical composition of water-treatment sludge was 28.79% Al2O3 and 27.06% SiO2. The zeolites were synthesized by merely employing the water-treatment sludge as silica and alumina sources without additional chemicals. Zeolite crystals synthesized through the water-treatment sludge were confirmed as an A-type zeolite structure. Zeolite A had the highest crystallinity obtained from a gel with the molar composition 2.1Na2O-Al2O3-1.6SiO2-65H2O after 5 h at a temperature of 90 ℃. The specific surface area of zeolite obtained was 55 ㎡ g-1, which was higher than commercial zeolite A. The removal efficiency of nitrogen in ammonia was 68% after 3 h of reaction time, while the removal efficiencies of Pb2+ and Cd2+ ions were 99.1% and 99.3%, respectively. These results indicate active ion exchange between Pb2+ or Cd2+ ion and Na+ ion in the zeolite framework. The adsorption experiments on the different zeolite addition conditions were performed for 3 h with 300 ppm humic acid. Based on the results, TOC's highest efficiency was 83% when 5 g of zeolite was added.

• Journal of the Korean Ceramic Society
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• v.18 no.2
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• pp.91-98
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• 1981

Synthetic zeolite A was prerared from domestic Hadong kaolin with sodium hydroxide solution and their ion exchange isotherms of $K^+$, $NH^{4+}$, $Li^+$ and $Ag^+$ ion were presented. The optimum reaction conditions for synthetic zeolite A from calcinated kaolin were 2 fold excess of 2N sodium hydroxide solution, 10$0^{\circ}C$ and 8 hours. It was observed that before the crystallization of zeolite A the samples reacted with sodium hydroxide solution had rather higher ion exchange capacities than zeolite A. The $K^+$-$Na^+$ and $Ag^+$$Na^+$ ion exchange isotherms were signoidal. The initial selectivity series was in the order $Ag^+$$K^+$>$Na^+$>$NH_4$>$Li^+$. Between approximately 33 and 67% replacement of soium ions the selectivity series became $Na^>$ and above 67% became $Ag^+$>$K^+$. Evidence were also presented to demonstrate that 8 out of 12 sodium ions per pseudo unit cell were not easily replaceable by lithium ions and 4 out of 12 not easily replaceable by ammonium ions.

• Membrane Journal
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• v.24 no.4
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• pp.285-291
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• 2014

The PTMSP[Poly(1-trimethylsilyl-1-propyne)]-NaY zeolite composite membranes were prepared by adding 0~50 wt% NaY zeolite to PTMSP. In order to investigate the characteristics of these membranes, we used the analytical methods such as FT-IR, $^1H$-NMR, GPC, DSC, TGA, and SEM. Gas permeation experiments were carried out at $23{\sim}26^{\circ}C$, $2kgf/cm^2$, and the permselectivity of $H_2$ and $N_2$ gases through the composite membranes was studied as a function of the NaY zeolite contents. According to TGA measurements, when NaY zeolite was inserted within the PTMSP, thermal stability of PTMSP was enhanced. Based on SEM observation, NaY zeolite was dispersed in the PTMSP-NaY zeolite composite membrane with a size of $1.5{\mu}m$. The permeability of $H_2$ and $N_2$ through the PTMSP-NaY zeolite composite membranes increased as NaY zeolite content increased. On the contrary, the selectivity($H_2/N_2$) of the PTMSP-NaY zeolite composite membranes decreased as zeolite content increased.

• Bulletin of the Korean Chemical Society
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• v.11 no.5
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• pp.407-410
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• 1990

Three binary ion-exchange isotherms of zeolite A have been determined using 0.1 M solutions of the aqueous nitrates for the one-step preparation of particular mixed-cation zeolite A compositions. Analyses were done primarily by flame emission spectrometry (FES), together with crystallographic determinations of $Cs^+$ and colorimetric determinations of $NH_{4^+}$. Corrections for a presumed impurity of extra-lattice species in powder sample were made for the determination of $Na^+$. The $Cs^+-Ag^+$ isootherm indicates a strong selectivity for $Ag^+$ through the entire range of zeolite composition. The $Ag^+-Na^+$ isotherm agrees very closely with that reported by Sherry and Walton, and that of $NH_{4^+}-Na^+$ resembles those obtained using zeolite pellets.